Poly-omic Predictors of Symptom Duration and Recovery for Adolescent Concussion

Concussion, Mild Clinical Trial

Official title: Poly-omic Predictors of Symptom Duration and Recovery for Adolescent Concussion

Status Recruiting

Clinical Trial Summary

The purpose of this study is to identify changes in salivary micro ribonucleic acid (miRNA) levels that are predictive of symptom duration and character following mild traumatic brain injury (mTBI) in children.

Clinical Trial Description

The objective of this multi-center study is to refine and validate a saliva RNA assessment for adolescent concussion, yielding a non-invasive test that predicts duration and character of symptoms, and helps guide clinical decisions. To accomplish this goal, the study will enroll 750 adolescents with mTBI. Saliva RNA levels and symptoms will be assessed at <48 hours, 7 days, and 30 days post-injury. Aim 1 will assess the ability of saliva RNA dynamics (Δ from <48 hours to day 7) to predict PPCS 30 days after mTBI (defined by persistence of ≥3 symptoms on day 30, compared with pre-injury state on the Post-Concussion Symptom Inventory; PCSI). RNA accuracy will be compared to a validated clinical prediction tool (5p tool). Aim 2 will assess the ability of saliva RNA dynamics (Δ from <48 hours to day 30) to identify recovered participants on day 30. RNA accuracy will be compared to change in composite score on a standardized reaction time test (from <48hrs to day 30). Completion of these aims will yield an objective biologic test that can be used for prognosis at the time of mTBI, and to aid clinical decisions regarding return-to-learn or return-to-play. ;

Related Conditions & MeSH terms

• Brain Concussion
• Concussion, Mild

• NCT number: NCT04582682
• Study type: Observational
• Source: Milton S. Hershey Medical Center
• Contact: Steven Hicks, MD, PhD
• Phone: 7175318006
• Email: shicks1@pennstatehealth.psu.edu
• Status: Recruiting
• Start date: January 18, 2021
• Completion date: January 2026